raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:716466

Rare isolated progressive retinal vasculopathy

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enRare isolated progressive retinal vasculopathy
frVasculopathie rétinienne isolée progressive rare
deSeltene isolierte progrediente retinale Vaskulopathie
esVasculopatía retiniana progresiva aislada rara
itVasculopatia retinica progressiva isolata rara
nlZeldzame geïsoleerde progressieve retinale vasculopathie
ptRare isolated progressive retinal vasculopathy
plRzadka izolowana postępująca waskulopatia siatkówki
csRare isolated progressive retinal vasculopathy
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card